Abnormality of nervous system morphology

Symptom Information:

Symptom ID: HPO:0012639
Cross references:
Is a (Direct Parents):
HPO         Abnormal neuron morphology
HPO         Abnormality of the nervous system
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the nervous system(HPO:0000707)
          Abnormality of nervous system morphology(HPO:0012639)
Database Frequency: 25 / 7739

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
5q14.3 microdeletion syndrome (Orphanet:228384)
6p22 microdeletion syndrome (Orphanet:251046)
6q25 microdeletion syndrome (Orphanet:251056)
Aplasia cutis - myopia (Orphanet:1117)
Arthrogryposis - hyperkeratosis, lethal form (Orphanet:1485)
CHARGE syndrome (Orphanet:138)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Chronic intestinal pseudo-obstruction (Orphanet:2978)
Craniofacial conodysplasia (Orphanet:85168)
Dermatoleukodystrophy (Orphanet:1659)
Ehlers-Danlos syndrome with periventricular heterotopia (Orphanet:82004)
Fanconi anemia (Orphanet:84)
Glutaryl-CoA dehydrogenase deficiency (Orphanet:25)
Holoprosencephaly (Orphanet:2162)
Lethal multiple pterygium syndrome (Orphanet:33108)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Mucolipidosis type 2 (Orphanet:576)
Neu-Laxova syndrome (Orphanet:2671)
Papilloma of choroid plexus (Orphanet:2807)
Peroxisomal acyl-CoA oxidase deficiency (Orphanet:2971)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Williams syndrome (Orphanet:904)